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Publication numberUS3845126 A
Publication typeGrant
Publication dateOct 29, 1974
Filing dateSep 25, 1967
Priority dateSep 29, 1966
Also published asDE1668610A1
Publication numberUS 3845126 A, US 3845126A, US-A-3845126, US3845126 A, US3845126A
InventorsR Giraudon, J Metivier
Original AssigneeRhone Poulenc Sa
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Benzaldoxime derivatives
US 3845126 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

United States Patent Int. (:1. cine 131/00 US. Cl. 260-566 AE 7 Claims ABSTRACT OF THE DISCLOSURE Benzaldoxime derivatives of the formula:

N02 wherein R represents hydrogen or alkyl of 1 through 3 carbon atoms, and

represents phenyl or phenyl carrying at least one member of the class consisting of halogen and alkyl of 1 through 3 carbon atoms, possess insecticidal and acaricidal properties.

This invention relates to new benzaldoxime derivatives, to processes for their preparation, and compositions containing them.

The new benzaldoxime derivatives of the present invention are those of the general formula:

No: I

wherein R represents a hydrogen atom or an alkyl group containing 1 to 3 carbon atoms, and R represents a hydrogen atom or one or more members of the class consisting of halogen atoms and alkyl groups containing 1 to 3 carbon atoms.

According to a feature of the invention, the aforesaid benzaldoxime derivatives are prepared by the reaction of an oxime of the formula:

mQ-onmv-on N01 II wherein R is as hereinbefore defined, with a benzyl halide of the formula:

formula:

III

3,845,126 Patented Oct. 29, 1974 (wherein R is as hereinbefore defined) by the usual methods for the halogenation of side chains of araliphatic hydrocarbons, or by halogenomethylation of benzene compounds of the formula:

wherein R is as hereinbefore defined.

According to another feature of the invention, the benzaldoxime derivatives of formula I are prepared by the reaction of an oxyamine of the formula:

R2 VI wherein R is as hereinbefore defined, with a benzylaldehyde of the formula:

1 102 VII wherein R is as herein-before defined. The reaction is effected in the absence or presence of an inert organic solvent, advantageously at a temperature of from 15 to C., and optionally in the presence of an alkaline condensing agent.

The oxyamine starting materials of formula VI can be obtained by the method described by P. Mamalis et al., J. Chem. Soc., p. 229 (1960).

The benzaldoxime derivatives of formula I possess remarkable insecticidal properties, especially against Musca domestica and Tribolium, and acaricidal properties, particularly against Tetranychus urticae, with a marked ovicidal activity. Preferred benzaldoxime derivatives of the invention are O-(3-chlorobenzyl)-3-nitrobenzaldoxime and the corresponding 3-bromobenzyl, 2-fiuorobenzyl and 3,4- dichlorobenzyl compounds and, more especially, O-(3- fluorobenzyl)-3-nitrobenzaldoxime, O (2-methylbenzyl)- 3-nitrobenzaldoxime and O-(2-chlorobenzyl)-4-methyl-3 nitrobenzaldoxime.

According to a further feature of the present invention there are provided pesticidal compositions containing at least one benzaldoxime derivative of formula I in association with one or more diluents compatible with the benzaldoxime and suitable for use in agricultural pesticidal compositions. Preferably, the compositions contain between 0.005 and by weight of benzaldoxime. The compositions may be solid if there is employed a powdered solid compatible diluent such as talc, calcined magnesia, kieselguhr, tricalcium phosphate, powdered cork, absorbent charcoal, or a clay such as kaolin or bentonite. Instead of a solid diluent, there may be used a liquid in which the benzaldoxime is dissolved or dispersed. The compositions may thus take the form of suspensions, emulsions or solutions in organic or aqueous-organic media, for example aromatic hydrocarbons (such as toluene, xylene), acetophenone, o-dichlorobenzene or mineral, animal or vegetable oils, or mixtures of these diluents. The compositions in the form of suspensions, emulsions or solutions may contain wetting, dipersing or emulsifying agents of the ionic or non-ionic type, for example sulphoricinoleates, quaternary ammonium derivatives or products based on condensates of ethylene oxide, such as the condensates of ethylene oxide with octylphenol, or fatty acid esters of anhydrosorbitols which have been rendered soluble by etherification of the free hydroxyl groups by condensation with ethylene oxide. It is preferable to use agents of the non-ionic type because they are not sensitive to electrolytes. When desired, emulsions of the benzaldoximes may be used in the form of self-emulsifying concentrates containing the active substance dissolved in the emulsifying agents or in a solvent containing an emulsifying agent compatible with the benzaldoxime and solvent, a simple addition of water to such concentrates producing compositions ready for use.

The solid compositions are preferably prepared by grinding the benzaldoxime with the solid diluent, or by impregnating the solid diluent with a solution of the benzaldoxime in a volatile solvent, evaporating the solvent, and if necessary grinding the product so as to obtain a powder, and may optionally incorporate a wetting or dispersing agent, for example of the types hereinbefore described.

The benzaldoxime derivatives of formula I are preferably employed for pesticidal purposes in a quantity of from to 150 g. of active substance per hectolitre of water, but lower concentrations may also be used.

The following Examples illustrate the invention.

EXAMPLE I A 2.3 N solution of potassium ethoxide in ethanol (21.6 cc.) is added to a suspension of S-nitrobenzaldoxime (8.3 g.) in ethanol (50 cc.), and then a solution of 3-chlorobenzyl bromide (10.3 g.) in ethanol (20 cc.) is added dropwise to the limpid solution obtained during the course of about 10 minutes. When the exothermic reaction is complete, the mixture is heated under reflux for 2 hours. After cooling, the potassium bromide precipitate is filtered off. The solvent is evaporated, and the residual oil g.) is distilled under reduced pressure to yield O-(3-chlorobenzyl)-3-nitrobenzaldoxime (10.2 g.), boiling at 200-205 C./0.2 mm. Hg with a melting point (capillary) of 42 C.

3-Chlorobenzyl bromide (boiling point 117-118 C./ mm. Hg) employed as starting material is prepared by bromination of 3-chloroto1uene.

The products of formula I specified in the following Table, in which the position of substituents on the benzene rings is indicated, were prepared by the procedure described in the foregoing Example starting with appropriate compounds of formulae II and III.

To 20 g. of O-(3-chlorobenzyl)-3-nitrobenzaldoxime are added 5 g. of a condensation product of octylphenol and ethylene oxide in the ratio of 10 molecules of ethylene oxide per molecule of octylphenol, and a mixture of equal volumes of toluene and acetophenone to make the volume up to 100 cc.

After suitable dilution with water, the solution obtained is used to destroy acarids. Depending on the desired effect, concentrations of 10 to 150 g. of active material per hectolitre give good results.

EXAMPLE III 400 g. of kaolin, 100 g. of ground gum arabic and 100 g. of calcium lignosulphite are added to 400 g. of O-(3,4- dichlorobenzyl)-3-nitrobenzaldoxime. After grinding and screening, the resulting powder, after dilution with water at the rate of 250 g. of powder per 100' litres of water, is used to protect plants against attack by acarids.

The acaricidal activity of benzaldoxime derivatives of general formula I is demonstrated by the following test:

Cotyledonous leaves of bean plants are dipped for 10 seconds in the emulsions to be studied. After drying, they are infested with red spiders. The fatalities are recorded 4 days after introducing the parasites.

The emulsifiable solutions used have the following composition:

Active product "I g l Cemulsol C- cc 0.2 Scurol O cc 0.2 o-Dichlorobenzene cc 1 Acetopheuone sufficient to make up to 5 cc.

Aqueous emulsions containing 0.2%, 0.1% and 0.05% of benzaldoxime derivatives are then prepared.

The results obtained are given in the following table.

1. Benzaldoxime derivative of the formula:

I R: N02

wherein R represents hydrogen or alkyl of 1 through 3 carbon atoms and represents phenyl carrying one or two halogens.

2. The benzaldoxime derivative according to claim 1 wherein R is hydrogen and R is fluorine in the 3-position of the benzene ring.

3. The benzaldoxime derivative according to claim 1 wherein R is methyl and R is chlorine in the 2-position of the benzene ring.

4. The benzaldoxime derivative according to claim 1 wherein R is hydrogen and R is chlorine in the 3-position of the benzene ring.

5. The benzaldoxime derivative according to claim 1 wherein R is hydrogen and R is bromine in the 3-position of the benzene ring.

6. The benzaldoxime derivative according to claim 1 wherein R is hydrogen and R is fluorine in the 2-position of the benzene ring.

7. The benzaldoxime derivative according to claim 1 wherein R is hydrogen and R: is 3,4-dichlorophenyl.

References Cited FOREIGN PATENTS 964,721 7/1964 Great Britain 260--566 LEON ZITVER, Primary Examiner G. A. SCHWARTZ, Assistant Examiner US Cl. X.R.

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4079149 *Jun 30, 1977Mar 14, 1978Shell Oil CompanyBenzyl oxime ethers
US4192893 *Dec 12, 1977Mar 11, 1980U.S. Philips CorporationAnti-depressive compounds
US4216329 *Jun 26, 1975Aug 5, 1980Philip Morris IncorporatedMethod of producing γ-amino alcohols
US4263227 *May 14, 1979Apr 21, 1981Ppg Industries, Inc.5-(2-Chloro-4-trifluoromethyl)-, or (4-trifluoromethyl or 2,6-dichloro-4-trifluoromethylphenoxy)-2-nitro-substituted carbonyl oxime-O-alkyl ethers
US4375981 *Nov 21, 1980Mar 8, 1983Ppg Industries, Inc.Method for controlling weed growth using herbicidally 5-(2-chloro-4-trifluoromethyl)-, or (4-trifluoromethyl or 2,6-dichloro-4-trifluoromethylphenoxy)-2-nitro-substituted carbonyl oxime-O-alkyl ethers
US5684200 *Dec 17, 1993Nov 4, 1997Basf AktiengesellschaftProcess for the preparation of hydroxylamine ethers and their salts and intermediates for this purpose
USRE30634 *Aug 27, 1979Jun 2, 1981Shell Oil CompanyBenzyl oxime ethers
EP0024888A2 *Aug 21, 1980Mar 11, 1981Rhone-Poulenc Inc.Ketoximinoether insecticides
WO1986000894A1 *Jul 22, 1985Feb 13, 1986Commw Scient Ind Res OrgOxime insecticides
Classifications
U.S. Classification564/256
International ClassificationA01N
Cooperative ClassificationA01N35/10
European ClassificationA01N35/10